首页> 外文期刊>Materials science & engineering, C. Materials for Biogical applications >Synthesis and characterization of amphiphilic block polymer poly(ethylene glycol)-poly(propylene carbonate)-poly(ethylene glycol) for drug delivery
【24h】

Synthesis and characterization of amphiphilic block polymer poly(ethylene glycol)-poly(propylene carbonate)-poly(ethylene glycol) for drug delivery

机译:两亲嵌段聚合物聚(乙二醇)-poly(丙二醇)-poly(乙二醇)对药物递送的合成与表征

获取原文
获取原文并翻译 | 示例
           

摘要

A novel amphiphilic block polymer poly(ethylene glycol)-poly(propylene carbonate)-poly(ethylene glycol) (PEG-PPC-PEG) was synthesized via the dicyclohexylcarbodiimide condensation reaction of double PEG-bis-amine and HOOC-PPC-COOH. The obtained copolymer was characterized by NMR to determine its structure. Using the PEG-PPC-PEG as the carrier and using doxorubicin (DOX) as a model drug, DOX-loaded nanoparticles with core shell structure were synthesized by self-assembly in water. The nanoparticles properties such as particle size, drug loading, encapsulation efficiency (EE) and drug release behavior were investigated as a function of the hydrophobic block length of PPC segments and compared with each other. The results showed that the EE was up to 88.8%. Nanoparticles were found to have a certain effect on the controlled release of DOX.
机译:通过双PEG-BIS-胺和HOOC-PPC-COOH的二氯己基二酰胺缩合反应合成了一种新型两亲嵌段聚合物聚(乙二醇)-Pold(碳酸亚乙二醇) - 聚(乙二醇)(乙二醇)(PEG-PPC-PEG)。 所得共聚物的特征在于NMR以确定其结构。 使用PEG-PPC-PEG作为载体并使用DOXORUBICIN(DOX)作为模型药物,通过在水中自组装合成具有核壳结构的DOX负载纳米颗粒。 作为PPC段的疏水块长度的函数研究了粒度,药物负载,包封效率(EE)和药物释放行为的纳米颗粒特性,并彼此比较。 结果表明,EE高达88.8%。 发现纳米颗粒对DOX的控释具有一定影响。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号